Criteria Flashcards

1
Q

NYHA functional classification for CHF: general

A

measure of severity of heart failure

Class I - mild
Class II - mild
Class III - moderate
Class IV - severe

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2
Q

NYHA functional classification for CHF: class i

A

Mild
Patients with cardiac disease but without resulting in limitation of physical activity.
Ordinary physical activity does not cause undue fatigue, palpitation (rapid or pounding heart beat), dyspnea (shortness of breath), or anginal pain (chest pain).

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3
Q

NYHA functional classification for CHF: class ii

A

mild
Patients with cardiac disease resulting in slight limitation of physical activity.
They are comfortable at rest.
Ordinary physical activity results in fatigue, palpitation, dyspnea, or anginal pain

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4
Q

NYHA functional classification for CHF: class iii

A

moderate
Patients with cardiac disease resulting in marked limitation of physical activity.
They are comfortable at rest.
Less than ordinary activity causes fatigue, palpitation, dyspnea, or anginal pain.

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5
Q

NYHA functional classification for CHF: class iv

A

Severe
Patients with cardiac disease resulting in the inability to carry on any physical activity without discomfort.
Symptoms of heart failure or the anginal syndrome may be present even at rest.
If any physical activity is undertaken, discomfort is increased.

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6
Q

What is CHADS2VASC score used for?

A

used determine the treatment plan with patients that have atrial fibrillation

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7
Q

What do you do for the different CHADS2VASC scores?

A

0 aspirin or no antithrombotic
1 aspirin or anticoagulation (warfarin)
2+ These patients are typically put on heparin and bridged with warfarin to an INR of 2-3

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8
Q

USPSTF Screening recommendations

A

REVIEW

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9
Q

when is AAA screening recommended?

A

one-time screening abdominal US indicated in all men of 65-75 years of age who have ever smoked

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10
Q

TIMI risk score for unstable angina and NSTEMI: general

A

Estimates mortality for patients with unstable angina and non-ST elevation MI.

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11
Q

TIMI risk score for unstable angina and NSTEMI: factors/scoring

A
All one point:
Age ≥65
≥3 CAD risk factors
--- (Hypertension, hypercholesterolemia, diabetes, family history of CAD, or current smoker)
Known CAD 
--- (stenosis ≥50%)
ASA use in past 7 days
Severe angina
--- (≥2 episodes in 24 hrs)
EKG ST changes ≥0.5mm
Positive cardiac marker
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12
Q

TIMI risk score for unstable angina and NSTEMI: interpretation

A

Patients with a score of 0 or 1 point are at lower risk of adverse outcome (death, MI, urgent revascularization) compared to patients with a higher risk score. However, the risk is not zero.

Patients with a higher risk score may require more aggressive medical or procedural intervention.

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13
Q

Duke criteria for infectious endocarditis: general

A

Diagnostic criteria for endocarditis.

Consists of pathological criteria, major clinical criteria, and minor clinical criteria

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14
Q

Duke criteria for infectious endocarditis: pathological criteria

A

If either is positive, diagnosis is definite:

Microorganisms in a vegetation
— Demonstrated by culture or histologic examination of a vegetation, a vegetation that has embolized, or an intracardiac abscess specimen.

Pathologic Lesions
— Vegetation or intracardiac abscess confirmed by histologic examination showing active endocarditis.

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15
Q

Duke criteria for infectious endocarditis: major criteria

A

If both are positive, diagnosis is definite:

Blood cultures positive for endocarditis
— Typical microorganisms consistent with IE from 2 separate blood cultures, microorganisms consistent with IE from persistently positive blood cultures, single positive blood culture for Coxiella burnetii or antiphase I IgG antibody titer >1:800.

Evidence of endocardial involvement
— Echocardiogram positive for IE, abscess, new partial dehiscence of prosthetic valve, new valvular regurgitation. Note: Worsening or changing of pre-existing murmur NOT sufficient.

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16
Q

Duke criteria for infectious endocarditis: minor criteria

A

If all are positive, diagnosis is definite:

Predisposing heart condition or injection drug use
Fever
Vascular phenomena
— Major arterial emboli, septic pulmonary infarcts, mycotic aneurysm, intracranial hemorrhage, conjunctival hemorrhages, and Janeway’s lesions.

Immunologic phenomena
— Glomerulonephritis, Osler’s nodes, Roth’s spots, and rheumatoid factor.

Microbiological evidence
— Positive blood culture but does not meet a major criterion as noted above or serological evidence of active infection with organism consistent with IE.

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17
Q

Child’s classification to assess severity of liver disease

A

https://www.2minutemedicine.com/the-child-pugh-score-prognosis-in-chronic-liver-disease-and-cirrhosis-classics-series/

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18
Q

Jones criteria for acute rheumatic fever: general

A

Diagnostic :

1 Required Criteria and 2 Major Criteria and 0 Minor Criteria
OR
1 Required Criteria and 1 Major Criteria and 2 Minor Criteria

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19
Q

Jones criteria for acute rheumatic fever: required criteria

A

Evidence of antecedent Strep infection: ASO / Strep antibodies / Strep group A throat culture / Recent scarlet fever / anti-deoxyribonuclease B / anti-hyaluronidase

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20
Q

Jones criteria for acute rheumatic fever: major criteria

A
Carditis
	Polyarthritis
	Chorea
	Erythema marginatum
	Subcutaneous Nodules
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21
Q

Jones criteria for acute rheumatic fever: minor criteria

A

Fever
Arthralgia
Previous rheumatic fever or rheumatic heart disease
Acute phase reactions: ESR / CRP / Leukocytosis
Prolonged PR interval

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22
Q

Light’s criteria for exudative pleural effusion: general

A

used to determine if pleural fluid is exudative (represents an alteration of the local factors that then precipitates a pleural fluid accumulation)

based on protein parameters and LDH parameters

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23
Q

Light’s criteria for exudative pleural effusion

A

Pleural fluid protein / Serum protein >0.5
Pleural fluid LDH / Serum LDH >0.6
Pleural fluid LDH > 2/3 * Serum LDH Upper Limit of Normal

24
Q

screening tests are used to diagnose diabetes mellitus

A

Fasting plasma glucose ­≥ 126 mg/dL,
random plasma glucose ≥ 200 mg/dL with symptoms (polyuria and polydipsia),
hemoglobin A1C ≥ 6.5%, or
a 2-hour plasma glucose ≥ 200 mg/dL after 75 gram oral glucose tolerance test.

These same test should be repeated to confirm the diagnosis unless signs of metabolic decompensation (diabetic ketoacidosis or hyperosmolar hyperglycemic state)

25
Q

CKD Staging

A
1	Normal or High	 > 90
 2	Mildly decreased	 60-89
 3 a	Mild to moderately decreased	45-59
 3 b	Moderate to severely decreased	30-44
 4	Severely decreased	15-29
 5	Kidney failure	< 15
26
Q

Behcet’s syndrome dx criteria

A

recurrent pathos ulcers (defined as at least 3 episodes within a 12-month period) plus two of the following:

Recurrent genital ulcers, commonly involving the scrotum in men and labia in women and sparing the glans penis and urethra. Ulcers commonly heal within 1-2 weeks with scarring.
Eye lesions, including anterior or posterior uveitis, hypopyon, retinal vasculitis, cystoid macular degeneration.
Skin lesions, including folliculitis, erythema nodosum, and/or acne-like exanthem.
Positive pathergy test, a diagnostic test that involves irritating the skin with a sterile needle. A positive result is marked by the formation of a erythematous papule 2 mm in diameter or larger that within 48 hours

27
Q

Normal: T-score

A

> -1 SD

28
Q

Osteopenia: T-score

A

< -1 and > -2.5

29
Q

Osteoporosis: T-score

A

< -2.5

30
Q

orthostatic hypotension

A

one or both of:
systolic 20mmHg
diastolic 10mmHg

within 2-5min of quiet standing after 5min supine rest

31
Q

lung cancer screening

A

annual screening for lung cancer with low-dose computed tomography in adults ages 55 to 80 years who have a 30 pack-year smoking history and currently smoke or have quit within the past 15 years.

Screening should be discontinued once a person has not smoked for 15 years or already gonna die

32
Q

GCS parameters

A

eye opening
verbal response
motor response

33
Q

GCS: eye opening points

A
1 = none
2 = response to pain
3 = response to verbal command
4 = spontaneous
34
Q

GCS: verbal response points

A
1 = none
2 = incomprehensible
3 = inappropriate words
4 = confused
5 = oriented
35
Q

GCS: motor response points

A
1 = none
2 = extension to pain (decerebrate)
3 = flexion to pain (decorticate)
4 = withdrawal to pain
5 = localizing to pain
6 = obey's commands
36
Q

Charcot’s triad components

A

RUQ pain
fever
jaundice

means ascending cholangitis

37
Q

Reynold’s pentad components

A

Charcot’s triad (RUQ pain, fever, jaundice)
+ hypotension
+ AMS

means ascending cholangitis

38
Q

3 most common AIDS-defining illnesses

A

(CD4<200 with)
pneumocystis pneumonia (40%)
cachexia in the form of HIV wasting syndrome (20%)
esophageal candidiasis

others:
opportunistic pathogens (coccidioidomycosis, cryptococcosis, cryptosporidiosis, disseminated CMV disease, refractory HSV infections, histoplasmosis, Mycobacterium tuberculosis, toxoplasmosis),
HIV encephalopathy, and
particular neoplasms (cervical cancer, Kaposi’s sarcoma, CNS lymphoma, Burkitt’s lymphoma)

39
Q

SIRS

A

2 or more of the following variables.

Fever of more than 38°C (100.4°F) or less than 36°C (96.8°F)
Heart rate of more than 90 beats per minute
Respiratory rate of more than 20 breaths per minute or arterial carbon dioxide tension (PaCO 2) of less than 32 mm Hg
Abnormal white blood cell count (>12,000/µL or < 4,000/µL or >10% immature [band] forms)

40
Q

Sepsis

A

SIRS with a source of infection

41
Q

Severe sepsis

A

sepsis with end-organ damage

confusion, hypotension systolic blood pressure < 90 mmHg or mean arterial pressure < 70 mmHg that responds to fluids

42
Q

Septic shock

A

persistent hypotension and perfusion abnormalities despite adequate fluid resuscitation

43
Q

What is Ann Arbor staging system

A

staging system for lymphomas, both in Hodgkin’s lymphoma and non-Hodgkin lymphoma .

44
Q

Stage options in Ann Arbor staging system

A
Stage I 	 
 Stage II 	  
Stage III	 
 Stage IV	 
 Sub-stage A	
 Sub-stage B
45
Q

Ann Arbor Stage I

A

Localized to a single lymph node or extralymphatic site

46
Q

Ann Arbor Stage II

A

Multiple lymph nodes or limited extralymphatic site on the same side of the diaphragm

47
Q

Ann Arbor Stage III

A

More than two sites on both sides of the diaphragm

48
Q

Ann Arbor Stage Iv

A

Diffuse or disseminated disease

49
Q

Ann Arbor Sub-stage A

A

No constitutional symptoms

50
Q

Ann Arbor Sub-stage B

A

Constitutional symptoms (fever, night sweats, weight loss)

51
Q

Hemorrhagic shock classes

A
  1. Class I hemorrhage involves a blood volume loss of up to 15% or approximately 750 cc of blood.
  2. Class II hemorrhage occurs when there is a 15 to 30% blood volume loss, approximately 750-1500 cc of blood,
  3. Class III hemorrhage involves a 30 to 40% blood volume loss, about 1500-2000 cc of blood
  4. Class IV involves more than 40% blood volume loss, greater than 2 liters of blood
52
Q

Sx of class I hemorrhagic shock

A

normal vital signs including heart rate, blood pressure, and pulse pressure,
may present with some anxiety.

53
Q

Sx of class II hemorrhagic shock

A

tachycardia (heart rate of 100 to 120/min), tachypnea (respiratory rate of 20 to 24/min), anxiety, and a normal systolic blood pressure with decreased pulse pressure. The skin may be cool and clammy, and capillary refill may be delayed.

54
Q

Sx of class III hemorrhagic shock

A

ignificant drop in systolic blood pressure and changes in mental status. Heart rate is increased (≥120/min ) and respiratory rate is also markedly elevated. Urine output is decreased and capillary refill is delayed.

55
Q

Sx of class IV hemorrhagic shock

A

significant decrease in blood pressure and mental status. Tachycardia is present often greater than 140/min. Urine output is minimal or absent. The skin is cold and pale, and capillary refill is delayed.

56
Q

Rome Criteria for IBS

A
  • All patients must experience at least 12 weeks or more (not necessarily consecutive) of abdominal discomfort or pain in the past year.
  • At least two of the three must accompany the pain: relief with bowel movements, onset associated with change in stool frequency, onset associated with change in stool appearance.
  • Patients may also experience passage of mucus, abdominal distension, or abnormal stool frequency, form, or passage.